Maha G. Alotaibi
Riyadh, 11671, Saudi Arabia
Last Updated: 09/26/2026
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Found 12 publications
Maternal-fetal transmission of Zika virus and long-term neurodevelopmental outcomes in children: a narrative review.
Journal: Translational pediatrics
Published: January 29, 2026
SLC25A42-Related Mitochondrial Disorder: New Cases and Literature Review.
Journal: Clinical genetics
Published: June 01, 2025
The relationship between practical skills confidence and readiness for transition to practice among nursing internship students: Exploring the mediating role of preceptorship.
Journal: Nurse education today
Published: September 05, 2024
Craniofacial and Dental Manifestations in Pediatric Patients with Achondroplasia: A Case Report and Clinical View.
Journal: International journal of clinical pediatric dentistry
Published: July 31, 2023
KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon.
Journal: Human genetics
Published: October 17, 2022
Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi Patient.
Journal: Case reports in pediatrics
Published: July 15, 2022
A Case of Geroderma Osteodysplasticum Syndrome: Unique Clinical Findings.
Journal: Global medical genetics
Published: October 15, 2021
Detection of a Recurrent TMEM38B Gene Deletion Associated with Recessive Osteogenesis Imperfecta.
Journal: Discoveries (Craiova, Romania)
Published: May 26, 2021
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathy.
Journal: Clinical genetics
Published: November 24, 2020
A de novo variant of CHD8 in a patient with autism spectrum disorder.
Journal: Discoveries (Craiova, Romania)
Published: April 21, 2020
Showing 1-12 of 12
Last Updated: 09/26/2026